Lupinus silvestres mexicanos como fuente de alcoloides quinolizidinicos de potencial económico
M.A. Ruiz-López1, P.M. García-López1, R. Rodríguez-Macías1, J.F. Zamora Natera1, M.L. Isaac-Virgen2, M. Múzquiz3,
1 Laboratorio de Biotecnología, Departamento de Botánica y Zoología, CUCBA. Universidad de Guadalajara. Carretera Guadalajara-Nogales Km 15.5 AP 1-139 Zapopan, Jalisco, México. Correo electrónico: mruiz@cucba.udg.mx
2 Instituto de Enfermedades Crónico-Degenerativas, Departamento de Fisiología, CUCS. Universidad de Guadalajara.
3 SGIT-INIA, Área de Tecnología de Alimentos, Apartado 811, 28080 Madrid, España.
]]>Recibido: 13 mayo 2009.
Aceptado: 8 diciembre 2009.
Abstract
Quinolizidine alkaloids such as lupanine, 13-hydroxylupanine, multiflorine, angustifoline and sparteine, which are present in the species of the genus Lupinus, have been reported to have biopesticide and pharmacological activities. The aim of this study was to quantify the content and variation of the individual alkaloids in seeds of L. mexicanus, L. exaltatus, L. montanus and L. stipulatus collected in different states of Mexico. Lupanine was the major (5.05 ± 0.37 mg/g) alkaloid found in L. mexicanus, whereas sparteine was the main alkaloid present in L. montanus (3.97 ± 0.49 mg/g). Conversely, L. stipulatus contained only small quantities of lupanine and sparteine (0.1 ± 0.002 and 0.04 ± 0.01 mg/g, respectively). Angustifoline was detected only in L. montanus, but in a very low amount (0.048 ± 0.03). The results of this study indicate that L. mexicanus and L. montanus can be considered as important sources of lupanine and sparteine for their use as natural pesticide or pharmacological agents.
Key words: L. mexicanus, L. exaltatus, L. montanus and L. stipulatus; lupanine, angustifoline, sparteine, 13-hydroxylupanine, angustifoline; biopesticide; pharmaceutical activity.
Resumen
Los alcaloides quinolizidinicos lupanina, 13-hidroxilupanina, multiflorina, angustifolina y esparteina, presentes en el género Lupinus poseen actividades bioplagicida y farmacológica. El objetivo del presente estudio fue cuantificar el contenido y variación de los alcaloides mencionados en semillas de L. mexicanus, L. exaltatus, L. montanus y L. stipulatus, colectados en diferentes estados de México. La lupanina fue el principal (5.05 ± 0.37mg /g) alcaloide encontrado en L. mexicanus, mientras que la esparteína fue el mayor alcaloide presente en L. montanus (3.97 ± 0.49 mg/g). Sin embargo, en L. stipulatus se encontraron pequeñas cantidades de lupanina y esparteína (0.1 ± 0.002 y 0.04 ± 0.01 mg/g, respectivamente). La angustifolina sólo se detectó en bajos niveles en L. montanus (0.048 ± 0.03). Los resultados de este estudio indican que L. mexicanus y L. montanus pueden ser considerados como una fuente importante de lupanina y esparteína, los cuales pueden ser utilizados como pesticidas o hipoglucémicos naturales.
]]> Palabras clave: L. mexicanus, L. exaltatus, L. montanus, L. stipulatus; lupanina, angustifolina, esparteína, 13-hidroxi-lupanine, angustifolina; bio-plaguicidas; actividad farmacéutica.
INTRODUCTION
The sweet lupin varieties Lupinus luteus, Lupinus angustifolius, and Lupinus albus with low alkaloid content, are recognized throughout the world as a potential source of high quality protein, fiber and fat (Lopez and Fuentes, 1991). However, they have lower adaptation and are preferred by a number of insects, bacteria, fungi, and herbivores (Wink, 1998), as compared to the alkaloid-rich wild type varieties.
The content and type of alkaloids found in different Lupinus species depend on the variety, habitat, phenology, plant organs (leaves, stems, flowers, pods, roots, and seeds) and weather conditions (Carey and Wink 1994; Gremigni et al., 2000; Christiansen. et al., 1997; Muzquiz et al., 1994a). The total content of quinolizidine alkaloids (QA) in seeds of lupin species ranges from 1.5% to 4.0% (Hatzold et al., 1983; Ruiz and Sotelo, 2001). In addition, more than 150 different QA's have been reported within this genus, of these, lupanine, multiflorine and sparteine have been found in both old and new world lupins (Wink et al., 1995). Sparteine was used in the treatment of cardiac arrhythmias and to induce uterine contractions. It has also been shown to depress the central nervous system and to have hypotensive, diuretic and anti-inflammatory activities (Schmeller and Wink, 1998; Szczawinska et al., 1994). The QA's lupanine, 13-hydroxylupanine and multiflorine have been reported to have pharmacological activities such as anticonvulsant, antipyretic and hypoglycemic (Hatzold et al., 1983; Kubo et al., 2006; García-López et al., 2004). Lupanine, 13-hydroxylupanine, angustifoline and sparteine were shown to have bactericide-like activity against Staphylococcus aureus, Bacillus subtilis, and Bacillus thuringiensis (De la Vega et al. , 1996). Lupanine and lupin alkaloid extracts have shown to have herbicidal activity, and the capacity to inhibit the growth of Fusarium avenaceum, Fusarium solani, Pythium aphanidermatum, Botrytis cinerea, Sclerotium rolfsii, Rhizoctonia solani, and Fusarium oxysporum (De la Cuadra et al., 1994; Muzquiz et al., 1994b Zamora et al., 2005; Zamora et al., 2008). Lupin alkaloids also have feeding deterrence effects on the red-legged earth mite Halotydeus destructor (Wang et al., 2000).
There are approximately 100 wild lupin species throughout Mexico, with the highest concentration being found in the "Sierra Madre Occidental" and "Eje Neovolcánico Transversal" (Bermudez et al., 2000). However, the alkaloid content or profile of some of these species is unknown and can be potentially use as natural products in agriculture and /or medicine.
The aim of this study was to determine the content and variability of lupanine, 13-hydroxylupanine, multiflorine, angustifoline and sparteine in seeds of L. exaltatus, L. montanus, L. stipulatus and L. mexicanus collected from several states and regions of Mexico.
MATERIAL AND METHODS
Seeds of several wild lupins were collected during the winter and spring of 2006 and 2007 at several locations in the Mexican states of Jalisco, Zacatecas, Mexico, and Guanajuato (table 1). The voucher specimens of L. exaltatus (No. 165321, 165435, 165641), L. montanus (No. 164989,164575, 172672), L. stipulatus (No. 178432) and L. mexicanus (No. 167885, 167890, 177884), were deposited in "Herbario del Instituto de Botánica, Universidad de Guadalajara (IBUG), Mexico.
]]> Seeds were separated, dried and ground to pass through a 150 mm sieve (Tecator, Cyclotec 1093). The alkaloid extraction was performed as described elsewhere (Muzquiz et al., 1993). One half gram of seed flour was homogenized in 5% trichloroacetic acid (3 x 5 mL) with a homogenizer and centrifuged at 3 000 r.p.m. for 5 min. After centrifugation, 1 mL of 10 M NaOH was added to the supernatant and the alkaloids were then extracted with dichloromethane (3 x 5 mL). The dichloromethane was evaporated and the alkaloids were dissolved in 1 mL of methanol. A 0.5 mL aliquot of the extract was added to 0.5 mL of a solution of codeine (internal standard) in methanol (2 mg/mL), each sample was diluted ten-fold.The samples were analyzed using a Perkin-Elmer Capillary Gas-Chromatograph, equipped with a phosphorous-nitrogen detector (PND) and Turbochrom for instrument control and data analysis. The samples were separated in an SPB-1 column (30 m x 0.25 mm i.d., 0.25-μm film thickness), using helium as the carrier gas (1.38 bar). The temperatures of the injector and detector were kept at 240°C and 300°C, respectively. The initial oven temperature was 150°C, with a temperature ramp of 5°C/min to 235°C, and finally held at 235°C for 15 minutes.
The alkaloid standards used were sparteine (Sigma, St Louis, MO, USA), lupanine perchlorate (Koch-Light, LTD, Conbrock, UK), 13-hydroxylupanine, multiflorine and angustifoline (isolated and kindly provided by Prof. Wysocka, University Adam Mickiewicz). Calibration curves were prepared for alkaloid standards; response was linear over a range of 0-1.250 mg/ml. The determination coefficient of alkaloid content was > 0.99. Alkaloids were identified by comparing retention times of standards with sample peaks.
RESULTS AND DISCUSSION
Table 2 shows the alkaloid concentration in seeds of the wild lupin species collected in different locations and times. As shown in this table, lupanine, sparteine, 13-hydroxylupanine, and multiflorine were present in all the samples collected. However, angustifoline was found only in L. montanus. Similar to the majority of American lupin species, angustifoline was not detected in L. exaltatus, L. stipulatus and L. mexicanus. The presence of angustifoline in L. montanus indicates a possible chemotaxonomic relationship of this species with the European lupins L. angustifolius, L. albus and L. polyphyllus that contain this alkaloid (Wink et al., 1995; Kinghorn et al., 1980). However, further analysis of other phytoconstituents would help to establish this relationship.
The lupanine was the major alkaloid in all lupin species with exception of L. montanus where sparteine was the principal alkaloid follow by lupanine. The average highest lupanine concentration was found in L. mexicanus followed by L. montanus, L. exaltatus, and L. stipulatus (5.05 ± 0.37, 1.65 ± 0.09, 1.47 ± 0.27, and 0.10 ± 0.002 mg/g, respectively). Although sparteine was detected in all lupins species the concentration was only significant in L. montanus (3.97 ± 0.49 mg/g). This level of sparteine in L. montanus is higher than that reported for L. reflexus (2.66 mg/g) and slightly lower than that of L. articus (4.31 mg/g) (Ruiz and Sotelo, 2001; Majak et al., 1994).
The minor alkaloids 13-hydroxylupanine and multiflorine were found in all lupins species with the highest content found in L. stipulatus, 0.12 and 0.2 mg/g, respectively.
A large variation in the average lupanine content among the lupin samples collected was observed, this could be due to differences among the species, locality, year of collection, and/or environmental conditions (Jansen, et al., 2009; Gremigni, et al., 2000; Christiansen. et al., 1997).
L. stipulatus was found to contain only small quantities of sparteine (0.04 ± 0.01 mg/g), lupanine (0.1 ± 0.002 mg/g), 13-hydroxylupanine (0.12 ± 0.004 mg/g) and multiflorine (0.2 ± 0.004 mg/g). Therefore, L. stipulatus is a poor source of these four alkaloids. Other peaks were observed in the chromatogram, however, additional gas chromatographic-mass spectrometry (GC-MS) and nuclear magnetic resonance analysis must be performed in order to determine if these are other alkaloids.
]]> The average highest concentration of 13-hydroxylupanine was found in L. stipulatus (0.12 ± 0.004 mg/g), followed by L. montanus (0.10 ± 0.09 mg/g), L. mexicanus (0.015 ± 0.018 mg/g) and L. exaltatus (0.015 ± 0.013 mg/g). The multiflorine content in L. mexicanus, L. exaltatus, L. montanus, and L. stipulatus was 0.096 ± 0.09, 0.004 ± 0.000, 0.07 ± 0.004, and 0.2 ± 0.004 mg/g, respectively. Even though these minor alkaloids posses biological activity their isolation and purification could be an expensive and time consuming process to purse.
CONCLUSIONS
The variability in the alkaloids content among species was larger than within individual species. L. mexicanus and L. montanus contain a high amount of lupanine and sparteine and can be a potential source of these alkaloids for agricultural and medical applications. Although, multiflorine and 13-hydroxylupanine have pharmacological activities, the isolation from these lupin species would be result impractical due to their low concentration.
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